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采用全外显子组测序进行全面的乳腺癌风险分析以及BRCA1和BRCA2突变与致癌性人乳头瘤病毒(HPV)的流行情况

Comprehensive breast cancer risk analysis with whole exome sequencing and the prevalence of and mutations and oncogenic HPV.

作者信息

Bumrungthai Sureewan, Duangjit Sureewan, Passorn Supaporn, Pongpakdeesakul Sutida, Butsri Siriwoot, Janyakhantikul Somwang

机构信息

Division of Biopharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Ubon Ratchathani University, Ubon Ratchathani 34190, Thailand.

Division of Microbiology and Parasitology, School of Medical Sciences, University of Phayao, Phayao 56000, Thailand.

出版信息

Biomed Rep. 2024 Aug 7;21(4):144. doi: 10.3892/br.2024.1832. eCollection 2024 Oct.

Abstract

Breast cancer is the most prevalent cancer and also the leading cause of cancer death in women worldwide. A comprehensive understanding of breast cancer risk factors and their incidences is useful information for breast cancer prevention and control planning. The present study aimed to provide information on single nucleotide polymorphisms (SNPs) and copy number variations (CNVs) in breast cancer, the allele frequency of two SNPs in breast cancer-related genes BRCA1 DNA repair associated ( rs799917) and ATP binding cassette subfamily G member 2 ( rs2231142), and the prevalence of human papillomavirus (HPV) infections in a normal population living in Phayao Province, Northern Thailand. One breast cancer and 10 healthy samples were investigated by whole exome sequencing (WES) and compared for genetic variation. The WES data contained SNPs in genes previously implicated in breast cancer and provided data on CNVs. The allele frequencies for SNPs rs799917 and rs2231142 were also examined. The SNP genotype frequencies were 35.88% CC, 46.54% CT, and 17.58% TT for rs799917 and 33.20% CC, 46.88% CA, and 19.92% AA for rs2231142. A total of 825 human whole blood samples were examined for HPV infection by PCR, and the pooled DNA was tested for HPV infection using metagenomic sequencing. No HPV infections were detected among all 825 samples or the pooled blood samples. The incidence of breast cancer among the tested samples was estimated based on acceptable breast cancer risk factors and demographic data and was 1.47%. The present study provided data on SNPs and CNVs in breast cancer-related genes. The associations between SNPs rs2231142 and rs799917 and breast cancer should be further investigated in a case-control study since heterozygous and homozygous variants are more common. Based on the detection of HPV infection in the blood samples, HPV may not be associated with breast cancer, at least in the Northern Thai population.

摘要

乳腺癌是全球女性中最常见的癌症,也是癌症死亡的主要原因。全面了解乳腺癌风险因素及其发生率,对于乳腺癌预防和控制规划而言是有用的信息。本研究旨在提供有关乳腺癌中单核苷酸多态性(SNP)和拷贝数变异(CNV)的信息、乳腺癌相关基因BRCA1 DNA修复关联基因(rs799917)和ATP结合盒亚家族G成员2(rs2231142)中两个SNP的等位基因频率,以及泰国北部帕尧府正常人群中人乳头瘤病毒(HPV)感染的患病率。通过全外显子组测序(WES)对1例乳腺癌样本和10例健康样本进行了研究,并比较了基因变异情况。WES数据包含先前与乳腺癌相关基因中的SNP,并提供了CNV数据。还检测了SNP rs799917和rs2231142的等位基因频率。rs799917的SNP基因型频率为CC型35.88%、CT型46.54%、TT型17.58%,rs2231142的SNP基因型频率为CC型33.20%、CA型46.88%、AA型19.92%。通过聚合酶链反应(PCR)对总共825份人类全血样本进行了HPV感染检测,并使用宏基因组测序对混合DNA进行了HPV感染检测。在所有825份样本或混合血样中均未检测到HPV感染。根据可接受的乳腺癌风险因素和人口统计学数据估算了检测样本中乳腺癌的发病率,为1.47%。本研究提供了乳腺癌相关基因中SNP和CNV的数据。由于杂合子和纯合子变异更为常见,因此SNP rs2231142和rs799917与乳腺癌之间的关联应在病例对照研究中进一步调查。基于血液样本中HPV感染的检测结果,HPV可能与乳腺癌无关,至少在泰国北部人群中如此。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bfa/11337157/a8083a56d1c2/br-21-04-01832-g00.jpg

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